Disease #05717 (COGIS (Cohen-Gibson syndrome (COGIS)), OMIM:617561)

Official abbreviation COGIS
Name Cohen-Gibson syndrome (COGIS)
OMIM ID 617561
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene EED
Associated tissues -
Disease features -
Remarks -
Date created 2020-04-06 13:49:36 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)

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